Lupus Foundation of America
@lupus
Lupus Foundation of America is the only national force devoted to solving the mystery of lupus while giving support to those who suffer from its brutal impact. 💜
➡️ Swipe to meet Rahul and Samantha, two athletes who turned their own races into something bigger for the #lupus community through Choose Your Own Race. Join them and turn an 5K, 10K, half marathon, marathon, triathlon or ultra into something charitable: buff.ly/zNAWE13
A new study explores the biomarker potential of IgG sugars for #lupus nephritis using a lectin-based test. Read the study: buff.ly/rgmlJLb
There's still time! Use the free SELF app for four days in July and you could receive a special gift from the LFA. Track medications, #lupus symptoms, or read the Activity of the Day. Supplies are limited! Start today: buff.ly/9zxFyWv
We're proud to announce Dr. Wobma from @harvardmed.bsky.social as the 2026 Michael Jon Barlin Pediatric Lupus Research Grant recipient. Her study explores using CAR-Treg therapy for immune balance and achieving drug-free remission in children with #lupus. Learn more: buff.ly/yn0QuMz
For many people, a barrier to participating in #lupusresearch is not knowing what to expect. ➡️ Swipe to learn about clinical trials, what participation looks like, and how your rights are protected. 🔗 Get involved in a trial today: buff.ly/OxV0dT7
Up to 80% of people with #lupus experience brain fog. A new tool, the Lupus Brain Fog Severity Scale, helps assess and track these cognitive symptoms. Read the study: buff.ly/NA6NNCp
DYK up to 60% of people with #lupus may experience #lupusnephritis? Lupus warrior and LFA Director of Care and Support Services Wendy Rodgers joined At the Table with Greg & Elliott to explain the importance of kidney health. Learn more: buff.ly/efMjr2n
What a weekend at #EssenceFest! 💜 Thank you to everyone who stopped by our booth, shared their stories, and kept the conversation going. ➡️ Swipe to see some of the moments we captured. Together, we keep fighting for everyone impacted by #lupus.
Today is #ChronicDiseaseAwarenessDay. 💜 #Lupus is a chronic autoimmune disease that can cause inflammation throughout the body. 9/10 people with lupus are women, and symptoms look different for everyone. Help us raise awareness and learn more: buff.ly/NR2aaog
Ready to get involved in #lupusresearch but not sure where to start? From the RAY® #Lupus Registry to the Lupus Clinical Trial Finder, there are tools designed to help you explore opportunities and make informed decisions. Learn more: buff.ly/yoSGP1O
Looking for a way to make an impact? 💜 ➡️ Swipe to see how our Purple for Purpose partners are turning everyday purchases into impact. A portion of every purchase goes directly to #lupus research, education, support and advocacy. Shop with purpose: buff.ly/aLEbXqA
📣 Nominations are still open for our Evelyn V. Hess Award and Mary Betty Stevens Young Investigator Prize. Whether they're an early-career or seasoned #lupus researcher, nominate someone who has made incredible contributions to #lupusresearch by 7/20: buff.ly/Qs8Cfcg #Medsky #Rheumsky
Do you live with #lupus, care for someone who does, and are 18+? We want to hear from you. Your responses are anonymous and will help shape the future of lupus care, education, and support. Take our online survey by 8/20 to share your experience: buff.ly/MgKDntd
Happy #NationalVideoGameDay! 🎮 DYK you can stream and play games anytime of the year to help end #lupus? Turn your stream into a fundraiser or join #GOTEL in May to raise money for lupus research, education and support programs 💜 Learn more: buff.ly/YGUc8br
We're proud to share that Lupus Science & Medicine, LFA's open-access journal, has achieved a 2025 Journal Impact Factor of 4.2, up from 4.0. We're also pleased to welcome four new members to our Editorial Board. Explore the latest #lupusresearch: buff.ly/NdZjTu2
Each breakthrough in #lupus treatment starts with people like you. Clinical trials are how new treatments are born, and every participant brings us closer to better options for everyone living with lupus. Find a trial near you: buff.ly/zDQKa96
👟 The #WalktoEndLupusNow is more than an event, it's community. Hear from our CEO Louise Vetter, #lupus warrior Kayla, and lupus advocate Lynn on what makes the day so meaningful to those living with and affected by lupus. Find a walk near you and join us: buff.ly/C4taAlH
☀️ DYK 40% to 70% of people with #lupus find that UV exposure makes their symptoms worse? From sunscreen to covering fluorescent bulbs with UV filters, there are steps you can take to protect yourself indoors and out. Learn more: buff.ly/zOUEu2N
Meet Brian. After hospitals stays and a #lupus nephritis diagnosis, he wondered why treatments weren't tailored to his symptoms. RAY, Research Accelerated by You, gave him a voice in changing that. Your experience matters. Join Brian and sign up today: buff.ly/9v80lhV
#FactFriday 💜 Up to 7 in 10 people with #lupus find that UV rays from sunlight or indoor lighting make their symptoms worse. Knowing how to protect yourself indoors and out is an important part of managing lupus. Learn tips for managing photosensitivity: buff.ly/gpYRvnu
☀️ July is #UVAwarenessMonth! For many people with lupus, UV exposure is a year-round challenge. It can trigger flares, skin rashes, fatigue, and joint pain, from both sunlight and artificial indoor lighting. Learn more and stay tuned all July for more sun safety tips: buff.ly/oTkTLUm
This July, we're highlighting ways the #lupus community can drive treatment forward: participating in #lupusresearch. Meet Beverly. After losing access to medication, she joined a trial and found it far more accessible than expected. Read her story: buff.ly/QO73JTE
Happy #WorldSocialMediaDay! 🌍💜 Social media has changed the way we connect and show up for each other. From raising awareness to finding support, our platforms are a space where #lupus warriors are never alone. Follow us across all our channels: buff.ly/szG6JH8
As #MensHealthMonth comes to a close, we're reminded that every man living with #lupus deserves access to the resources, community, and support that makes a difference. 💜 From support groups to expert insights and personalized guidance, read our blog: buff.ly/r9ALELk
⏰ Today is the LAST DAY to earn your customizable Walk to End Lupus Now baseball jersey! 👟 Raise $500 by midnight and wear it at your walk. Every dollar brings us closer to ending #lupus — don't miss out. Register today: buff.ly/GNN7jeP
We're proud to announce the 2026 Lupus Canada Catalyst Grant recipient, Dr. Knight. Her study will use a non-invasive brain imaging technology to understand cognitive dysfunction in children with #lupus to improve care and quality of life. 📖 Learn more: buff.ly/5aNLZWh
If your company has an employee matching gift program, you can maximize your support for the #lupus community throughout the year by doubling or even tripling your next donation to the Lupus Foundation of America! Visit our site to learn if your company has a similar program: buff.ly/0nqYhJr
💜🚨 48 hours left! Raise $500 by June 30 and earn your customizable #WalktoEndLupusNow baseball jersey. 👟 Cross that finish line wearing your name or your team while fighting to end #lupus. Get started today: buff.ly/GNN7jeP
😎 Today is #NationalSunglassesDay. For many #lupus warriors, sun protection is an everyday necessity. Up to 7 in 10 people with lupus have photosensitivity, meaning UV rays can trigger flares & other symptoms. Learn more about light sensitivity & lupus: buff.ly/vrgHtVn